The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126785451 12678545 1 I 20160727 20160801 20160823 20160823 PER US-PFIZER INC-2016370421 PFIZER 81.00 YR F Y 0.00000 20160823 OT US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126785451 12678545 1 PS TIKOSYN DOFETILIDE 1 Oral 250MCG ONE CAPSULSE TWICE A DAY L95145 20931 250 UG CAPSULE, HARD BID
126785451 12678545 2 C ELIQUIS APIXABAN 1 Oral 5MG ONE TABLET EVERY 12 HOURS 0 5 MG TABLET
126785451 12678545 3 C CARDIZEM DILTIAZEM HYDROCHLORIDE 1 Oral 120 MG, 1X/DAY 0 120 MG CAPSULE QD
126785451 12678545 4 C RYTHMOL PROPAFENONE HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126785451 12678545 1 Atrial fibrillation
126785451 12678545 2 Blood viscosity increased
126785451 12678545 3 Cardiac flutter

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126785451 12678545 Asthenia
126785451 12678545 Dizziness
126785451 12678545 Heart rate increased
126785451 12678545 Tremor

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126785451 12678545 1 20160726 0
126785451 12678545 2 20160726 0
126785451 12678545 3 2009 0
126785451 12678545 4 2009 0